Variant #0001015167 (NC_000014.8:g.74425926C>T, NM_182476.2:c.782C>T (COQ6))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.74425926C>T
DNA change (hg38) -
Published as COQ6(NM_182476.3):c.782C>T (p.P261L)
ISCN -
DB-ID COQ6_000031
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 5.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ENTPD5 NM_001249.2 +/. - c.*7705G>A r.(=) p.(=)
FAM161B NM_152445.2 +/. - c.-9008G>A r.(?) p.(=)
COQ6 NM_182476.2 +/. - c.782C>T r.(?) p.(Pro261Leu)


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